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Direct Covalent Coupling of Porphyrins to Graphene
Author(s) -
Daniela Dasler,
Ricarda A. Schäfer,
Martin B. Minameyer,
Jakob F. Hitzenberger,
Frank Hauke,
Thomas Drewello,
Andreas Hirsch
Publication year - 2017
Publication title -
journal of the american chemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.115
H-Index - 612
eISSN - 1520-5126
pISSN - 0002-7863
DOI - 10.1021/jacs.7b04122
Subject(s) - graphene , porphyrin , chemistry , covalent bond , raman spectroscopy , intercalation (chemistry) , graphite , fluorescence spectroscopy , mass spectrometry , spectroscopy , combinatorial chemistry , photochemistry , fluorescence , nanotechnology , organic chemistry , materials science , physics , chromatography , quantum mechanics , optics
Graphene-porphyrin nanohybrid materials with a direct covalent linkage between the graphene carbon network and the functional porphyrin unit have been successfully synthesized via a one-pot reductive diazotation approach. A graphite-potassium intercalation compound (KC 8 ) was dispersed in THF, and different isolated porphyrin-diazonium salts were added. The direct covalent binding and the detailed characterization of the functional hybrid material were carried out by Raman spectroscopy, TG-MS, UV/vis, and fluorescence spectroscopy. LDI-ToF mass spectrometry was introduced as a new versatile and sensitive tool to investigate covalently functionalized graphene derivatives and to establish the composition of the respective nanohybrid materials.

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